A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv685263



Internal ID15075229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:70839740..70842056hg38UCSC Ensembl
Innerchr10:72599497..72601813hg19UCSC Ensembl
Innerchr10:72269503..72271819hg18UCSC Ensembl
Innerchr10:72269503..72271819hg17UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg382317
hg192317
hg182317
hg172317
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517453
Supporting Variants
Samples
Known GenesSGPL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv685263
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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